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rs759072800

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs759072800(C;T)
Make rs759072800(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position44151069
GeneGCK
is asnp
is mentioned by
dbSNPrs759072800
ebirs759072800
HLIrs759072800
Exacrs759072800
Varsomers759072800
Maprs759072800
PheGenIrs759072800
hapmaprs759072800
1000 genomesrs759072800
hgdprs759072800
ensemblrs759072800
gopubmedrs759072800
geneviewrs759072800
scholarrs759072800
googlers759072800
pharmgkbrs759072800
gwascentralrs759072800
openSNPrs759072800
23andMers759072800
23andMe allrs759072800
SNP Nexus

SNPshotrs759072800
SNPdbers759072800
MSV3drs759072800
GWAS Ctlgrs759072800
Max Magnitude0
ClinVar
Risk rs759072800(T;T)
Alt rs759072800(T;T)
Reference rs759072800(C;C)
Significance Probable-Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene GCK
CLNDBN Maturity-onset diabetes of the young, type 2
Reversed 0
HGVS NC_000007.13:g.44190668C>T
CLNSRC
CLNACC RCV000193215.1,